Literature DB >> 21402750

Recognition of 5α-reductase-2 deficiency in an adult female 46XY DSD clinic.

Marta Berra1, Emma L Williams, Barbara Muroni, Sarah M Creighton, John W Honour, Gill Rumsby, Gerard S Conway.   

Abstract

CONTEXT: The late presentation of steroid 5α-reductase-2 (SRD5A2) deficiency in females is poorly characterised. The ratios of 5α/5β-reduced metabolites of adrenal steroids in a urine steroid profile (USP) can give an indication of SRD5A2 deficiency, although the diagnostic cut-off for 5α/5β ratios are not clearly defined in genetically confirmed cases.
OBJECTIVE: The aim of this study was to establish the frequency of SRD5A2 deficiency in an adult clinic for disorders of sexual development (DSD) focussing on 46XY partially virilised adult female subjects. We investigated the relationship between USP results and SRD5A2 genetic sequence and determined the cut-off for USP 5α/5β-reduced steroid ratios compared with gene sequencing for the identification of SRD5A2 deficiency.
METHODS: USP and SRD5A2 genetic analyses were performed in 23 adult females, aged 19-57 years, with 46XY DSD and in four males with confirmed SRD5A2 deficiency. 5α-Reductase activity was assessed using the USP ratio of androsterone to aetiocholanolone (A/Ae), 5α-tetrahydrocortisol (5α-THF)/tetrahydrocortisol (THF) and 5α-tetrahydrocorticosterone to tetrahydrocorticosterone (5α-THB/THB).
RESULTS: The SRD5A2 gene mutations were found in 10/23 (43%) females and in all four males. Totally, four novel mutations were identified. All mutation-positive subjects had A/Ae and 5α-THB/THB ratios below the lower limit of normal (100% sensitivity) while the sensitivity of 5α-THF/THF ratio was 90%.
CONCLUSION: SRD5A2 deficiency is more prevalent than expected in the adult female 46XY DSD population. The clinical spectrum of this disorder may extend to a more female phenotype than previously considered to include individuals with little or no virilisation.

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Year:  2011        PMID: 21402750     DOI: 10.1530/EJE-10-0930

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  10 in total

1.  Puberty reveals a familial disorder of sex development.

Authors:  A K Annamalai; A D Cluroe; E Sala; S M Park; J MacDougall; I A Hughes; H L Simpson
Journal:  Endocrine       Date:  2012-10       Impact factor: 3.633

2.  Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5-alpha reductase type 2 deficiency.

Authors:  Heather M Byers; Lauren H Mohnach; Patricia Y Fechner; Ming Chen; Inas H Thomas; Linda A Ramsdell; Margarett Shnorhavorian; Elizabeth A McCauley; Anne-Marie E Amies Oelschlager; John M Park; David E Sandberg; Margaret P Adam; Catherine E Keegan
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-05-25       Impact factor: 3.908

3.  Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene.

Authors:  Asma Deeb; Hana Al Suwaidi; Fakunle Ibukunoluwa; Salima Attia
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Review 4.  Integrative and Analytical Review of the 5-Alpha-Reductase Type 2 Deficiency Worldwide.

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Journal:  Appl Clin Genet       Date:  2020-04-14

Review 5.  Primary Amenorrhea Due to Anatomical Abnormalities of the Reproductive Tract: Molecular Insight.

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Journal:  Int J Mol Sci       Date:  2021-10-25       Impact factor: 5.923

6.  An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.

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7.  Loss of 5α-reductase type 1 accelerates the development of hepatic steatosis but protects against hepatocellular carcinoma in male mice.

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Journal:  Endocrinology       Date:  2013-09-30       Impact factor: 4.736

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Authors:  Jeffrey A French; Brett Frye; Jon Cavanaugh; Dongren Ren; Aaryn C Mustoe; Lisa Rapaport; Jennifer Mickelberg
Journal:  Biol Sex Differ       Date:  2016-06-02       Impact factor: 5.027

9.  Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD.

Authors:  Federica Buonocore; Oliver Clifford-Mobley; Tom F J King; Niccolò Striglioni; Elim Man; Jenifer P Suntharalingham; Ignacio Del Valle; Lin Lin; Carlos F Lagos; Gill Rumsby; Gerard S Conway; John C Achermann
Journal:  J Endocr Soc       Date:  2019-10-10

10.  Characterising SRD5A2 Gene Variants in 37 Indonesian Patients with 5-Alpha-Reductase Type 2 Deficiency.

Authors:  Nanis S Marzuki; Firman P Idris; Hannie D Kartapradja; Alida R Harahap; Jose R L Batubara
Journal:  Int J Endocrinol       Date:  2019-12-01       Impact factor: 3.257

  10 in total

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